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Items: 12

1.

Genomic imprinting at a boundary element flanking the SDHD locus.

Baysal BE, McKay SE, Kim YJ, Zhang Z, Alila L, Willett-Brozick JE, Pacak K, Kim TH, Shadel GS.

Hum Mol Genet. 2011 Nov 15;20(22):4452-61. doi: 10.1093/hmg/ddr376. Epub 2011 Aug 23.

2.

Identification of a 4.9-kilo base-pair Alu-mediated founder SDHD deletion in two extended paraganglioma families from Austria.

Janecke AR, Willett-Brozick JE, Karas C, Hasipek M, Loeffler-Ragg J, Baysal BE.

J Hum Genet. 2010 Mar;55(3):182-5. doi: 10.1038/jhg.2009.142. Epub 2010 Jan 29.

PMID:
20111059
4.

Common variations in ALG9 are not associated with bipolar I disorder: a family-based study.

Baysal BE, Willett-Brozick JE, Bacanu SA, Detera-Wadleigh S, Nimgaonkar VL.

Behav Brain Funct. 2006 Jul 21;2:25.

5.

Analysis of CHEK2 gene for ovarian cancer susceptibility.

Baysal BE, DeLoia JA, Willett-Brozick JE, Goodman MT, Brady MF, Modugno F, Lynch HT, Conley YP, Watson P, Gallion HH.

Gynecol Oncol. 2004 Oct;95(1):62-9.

PMID:
15385111
6.

An Alu-mediated partial SDHC deletion causes familial and sporadic paraganglioma.

Baysal BE, Willett-Brozick JE, Filho PA, Lawrence EC, Myers EN, Ferrell RE.

J Med Genet. 2004 Sep;41(9):703-9. No abstract available. Erratum in: J Med Genet. 2005 Jul;42(7):582.

7.

Altitude is a phenotypic modifier in hereditary paraganglioma type 1: evidence for an oxygen-sensing defect.

Astrom K, Cohen JE, Willett-Brozick JE, Aston CE, Baysal BE.

Hum Genet. 2003 Aug;113(3):228-37. Epub 2003 Jun 17.

PMID:
12811540
8.

A mannosyltransferase gene at 11q23 is disrupted by a translocation breakpoint that co-segregates with bipolar affective disorder in a small family.

Baysal BE, Willett-Brozick JE, Badner JA, Corona W, Ferrell RE, Nimgaonkar VL, Detera-Wadleigh SD.

Neurogenetics. 2002 Mar;4(1):43-53.

PMID:
12030331
9.

Prevalence of SDHB, SDHC, and SDHD germline mutations in clinic patients with head and neck paragangliomas.

Baysal BE, Willett-Brozick JE, Lawrence EC, Drovdlic CM, Savul SA, McLeod DR, Yee HA, Brackmann DE, Slattery WH 3rd, Myers EN, Ferrell RE, Rubinstein WS.

J Med Genet. 2002 Mar;39(3):178-83.

10.

Germ line insertion of mtDNA at the breakpoint junction of a reciprocal constitutional translocation.

Willett-Brozick JE, Savul SA, Richey LE, Baysal BE.

Hum Genet. 2001 Aug;109(2):216-23.

PMID:
11511928
11.
12.

Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma.

Baysal BE, Ferrell RE, Willett-Brozick JE, Lawrence EC, Myssiorek D, Bosch A, van der Mey A, Taschner PE, Rubinstein WS, Myers EN, Richard CW 3rd, Cornelisse CJ, Devilee P, Devlin B.

Science. 2000 Feb 4;287(5454):848-51.

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